AtlasKellele me abiks olemeMeie teadusTootedTulemused
Logi sisseKüsiSekveneeri oma genoom↗
Tunnus
Echoing another person's speech
Kliiniline nimetus: Echolalia
Echolalia is the automatic imitative repetition of sounds, words, or phrases in the absence of explicit awareness. The repeated words or phrases are typically odd or used in a non-social manner. These can be words or phrases that the affected individual has heard or invented.
Kokkuvõte
- Teised nimetused
- Echologia, Echophrasia, Repeated speech
- Kehasüsteem
- Abnormality of the nervous system
AtlasKellele me abiks olemeMeie teadusTootedTulemused
Logi sisseKüsiSekveneeri oma genoom↗
Selle lehe andmed
Lehe aadressile saab lisada .json või päringusse application/json, et lugeda seda JSON-vormingus.
library(jsonlite)
url <- "https://dantelabs.com/traits/echolalia.json"
page <- fromJSON(url)
page$trait$nameEchoing another person's speechHP:0010529
AtlasKellele me abiks olemeMeie teadusTootedTulemused
Logi sisseKüsiSekveneeri oma genoom↗
Lugege välja geenid, mis on seotud Echoing another person's speech-ga, ja kogu ülejäänud genoom ühe testiga.
Alates 449 $Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast
Telli oma Genome Test43 condition reports read genes linked to this trait
Dante Labs condition reports look at the genes behind groups of inherited conditions, read from one whole-genome test. Each page says which conditions and genes a report covers, how it is read and what it cannot tell you.
- Frontotemporal DementiaReads 7 of these genesCHMP2BGRNMAPTPSEN1SQSTM1VCPAbout this report →
- Birt-Hogg-Dubé SyndromeReads 1 of these genesFLCNAbout this report →
- CYLD Cutaneous SyndromeReads 1 of these genesCYLDAbout this report →
- Alzheimer diseaseReads 2 of these genesPSEN1TREM2About this report →
Show 39 more reports
- Intellectual DisabilityReads 12 of these genesCHD8EHMT1RAI1SMARCA2TCF4UBE2AAbout this report →
- Amyotrophic Lateral Sclerosis (ALS)Reads 4 of these genesCHMP2BSQSTM1VCPCYLDAbout this report →
- CitrullinemiaReads 1 of these genesSLC25A13About this report →
- Urea Cycle DisorderReads 2 of these genesSLC25A13NAGSAbout this report →
- Leukocyte Adhesion DeficiencyReads 1 of these genesSLC35C1About this report →
- Microphthalmia, Anophthalmia & ColobomaReads 3 of these genesCOX7BHCCSNDUFB11About this report →
- Adult-Onset Leukodystrophies (CSF1R, LMNB1, Nasu-Hakola)Reads 1 of these genesTREM2About this report →
- Familial Paget Disease of BoneReads 1 of these genesSQSTM1About this report →
- Congenital Myasthenic SyndromeReads 2 of these genesSNAP25PLECAbout this report →
- Autoimmune Lymphoproliferative Syndrome (ALPS)Reads 1 of these genesKRASAbout this report →
- Anterior Segment Dysgenesis, Axenfeld-Rieger Syndrome & AniridiaReads 1 of these genesITPR1About this report →
- Autism Spectrum DisorderReads 1 of these genesCHD8About this report →
- Kidney CancerReads 1 of these genesFLCNAbout this report →
- Urinary and Renal System TumourReads 1 of these genesFLCNAbout this report →
- Neuronal Ceroid LipofuscinosisReads 1 of these genesGRNAbout this report →
- OsteopetrosisReads 1 of these genesAMER1About this report →
- Parkinson DiseaseReads 1 of these genesMAPTAbout this report →
- Distal MyopathiesReads 1 of these genesVCPAbout this report →
- Epidermolysis BullosaReads 1 of these genesPLECAbout this report →
- Hereditary Corneal DystrophiesReads 1 of these genesTCF4About this report →
- Other Inherited LeukodystrophiesReads 2 of these genesTMEM106BTREM2About this report →
- Autoimmune DiseaseReads 1 of these genesKRASAbout this report →
- Noonan SyndromeReads 1 of these genesKRASAbout this report →
- Syndromic CraniosynostosisReads 1 of these genesFGFR1About this report →
- Congenital Disorders of GlycosylationReads 2 of these genesSLC35C1ATP6AP2About this report →
- Pelizaeus-Merzbacher Disease & Hypomyelinating LeukodystrophiesReads 1 of these genesTMEM106BAbout this report →
- VitreoretinopathyReads 1 of these genesCTNNB1About this report →
- Inherited ThrombocytopeniasReads 1 of these genesACTBAbout this report →
- Limb-Girdle Muscular DystrophyReads 1 of these genesPLECAbout this report →
- Autosomal Dominant Cerebellar Ataxias (SCAs and DRPLA)Reads 1 of these genesITPR1About this report →
- Dystonia, Myotonia, Paroxysmal DyskinesiaReads 1 of these genesACTBAbout this report →
- Epilepsy (Full Panel)Reads 2 of these genesSNAP25ATP6AP2About this report →
- Hypogonadotropic HypogonadismReads 1 of these genesFGFR1About this report →
- Lysosomal Storage DiseaseReads 1 of these genesGRNAbout this report →
- Hypertrophic CardiomyopathyReads 1 of these genesKRASAbout this report →
- Charcot-Marie-Tooth DiseaseReads 1 of these genesVCPAbout this report →
- Hearing Loss and DeafnessReads 1 of these genesACTG1About this report →
- Primary Mitochondrial DiseaseReads 1 of these genesNDUFB11About this report →
- Other Inborn Errors of ImmunityReads 1 of these genesKRASAbout this report →
Lugege välja geenid, mis on seotud Echoing another person's speech-ga, ja kogu ülejäänud genoom ühe testiga.
Alates 449 $Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast
Telli oma Genome Test47 geeni on seotud tunnusega Echoing another person's speech
Nende geenide muutused põhjustavad haruldasi haigusi, mille puhul esineb Echoing another person's speech. Enamikul selle tunnusega inimestest ei ole ühtegi neist haigustest. Selles loendis olev geen ei ütle midagi kellegi enda genoomi kohta.
| Geen | Kui sageli seda täheldatakse | Haigused |
|---|---|---|
| CHD8chromodomain helicase DNA binding protein 8 | Alati | Esineb 1 haiguses |
| FEM1Bfem-1 homolog B | Alati | Esineb 1 haiguses |
| ITPR1inositol 1,4,5-trisphosphate receptor type 1 | Alati | Esineb 1 haiguses |
| RNU6ATACRNA, U6atac small nuclear | Alati | Esineb 1 haiguses |
| SNAP25synaptosome associated protein 25 | Alati | Esineb 1 haiguses |
| UBAP2Lubiquitin associated protein 2 like | Alati | Esineb 1 haiguses |
| ACTBactin beta | Väga sageli (80–99%) | Esineb 1 haiguses |
| ACTG1actin gamma 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| CHMP2Bcharged multivesicular body protein 2B | Väga sageli (80–99%) | Esineb 1 haiguses |
| CKAP2Lcytoskeleton associated protein 2L | Väga sageli (80–99%) | Esineb 1 haiguses |
| EHMT1euchromatic histone lysine methyltransferase 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| GRNgranulin precursor | Väga sageli (80–99%) | Esineb 1 haiguses |
| MAPTmicrotubule associated protein tau | Väga sageli (80–99%) | Esineb 2 haiguses |
| PLECplectin | Väga sageli (80–99%) | Esineb 1 haiguses |
| PSEN1presenilin 1 | Väga sageli (80–99%) | Esineb 2 haiguses |
| RAI1retinoic acid induced 1 | Väga sageli (80–99%) | Esineb 2 haiguses |
| SMARCA2SWI/SNF related BAF chromatin remodeling complex subunit ATPase 2 | Väga sageli (80–99%) | Esineb 1 haiguses |
| SQSTM1sequestosome 1 | Väga sageli (80–99%) | Esineb 1 haiguses |
| TCF4transcription factor 4 | Väga sageli (80–99%) | Esineb 1 haiguses |
| TMEM106Btransmembrane protein 106B | Väga sageli (80–99%) | Esineb 1 haiguses |
| TREM2triggering receptor expressed on myeloid cells 2 | Väga sageli (80–99%) | Esineb 1 haiguses |
| VCPvalosin containing protein | Väga sageli (80–99%) | Esineb 1 haiguses |
| CYLDCYLD lysine 63 deubiquitinase | Sageli (30–79%) | Esineb 1 haiguses |
| FGFR1fibroblast growth factor receptor 1 | Sageli (30–79%) | Esineb 1 haiguses |
| KRASKRas proto-oncogene, GTPase | Sageli (30–79%) | Esineb 1 haiguses |
| MSL2MSL complex subunit 2 | Sageli (30–79%) | Esineb 1 haiguses |
| SLC35C1solute carrier family 35 member C1 | Sageli (30–79%) | Esineb 1 haiguses |
| UBE2Aubiquitin conjugating enzyme E2 A | Sageli (30–79%) | Esineb 2 haiguses |
| ADNPactivity dependent neuroprotector homeobox | Mõnikord (5–29%) | Esineb 1 haiguses |
| AMER1APC membrane recruitment protein 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| ATP6AP2ATPase H+ transporting accessory protein 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| COX7Bcytochrome c oxidase subunit 7B | Mõnikord (5–29%) | Esineb 1 haiguses |
| CTNNB1catenin beta 1 | Mõnikord (5–29%) | Esineb 1 haiguses |
| GRIK2glutamate ionotropic receptor kainate type subunit 2 | Mõnikord (5–29%) | Esineb 1 haiguses |
| HCCSholocytochrome c synthase | Mõnikord (5–29%) | Esineb 1 haiguses |
| KDM5Alysine demethylase 5A | Mõnikord (5–29%) | Esineb 1 haiguses |
| NDUFB11NADH:ubiquinone oxidoreductase subunit B11 | Mõnikord (5–29%) | Esineb 1 haiguses |
| PDZD8PDZ domain containing 8 | Mõnikord (5–29%) | Esineb 1 haiguses |
| PUF60poly(U) binding splicing factor 60 | Mõnikord (5–29%) | Esineb 1 haiguses |
| SLC25A13solute carrier family 25 member 13 | Mõnikord (5–29%) | Esineb 1 haiguses |
Näita veel 7 geeni
| Geen | Kui sageli seda täheldatakse | Haigused |
|---|---|---|
| KDM6Blysine demethylase 6B | Harva (1–4%) | Esineb 1 haiguses |
| NAGSN-acetylglutamate synthase | Harva (1–4%) | Esineb 1 haiguses |
| SPTBN1spectrin beta, non-erythrocytic 1 | Harva (1–4%) | Esineb 1 haiguses |
| FLCNfolliculin | Pole registreeritud | Esineb 1 haiguses |
| HDChistidine decarboxylase | Pole registreeritud | Esineb 1 haiguses |
| HERC2HECT and RLD domain containing E3 ubiquitin protein ligase 2 | Pole registreeritud | Esineb 1 haiguses |
| SLITRK1SLIT and NTRK like family member 1 | Pole registreeritud | Esineb 1 haiguses |
Kui sageli see esineb geenist tulenevate seisunditega inimeste seas, kõige sagedamini nende kõigi seas, nagu on märgitud Inimese fenotüübi ontoloogias. Need lehed kirjeldavad tunnuseid ja nende taga olevaid uuringuid; need ei ole diagnoos ning sümptomite kohta tuleks küsida arstilt või geneetilt nõustajalt.
Laiemad tunnused
Allikas
- Inimese fenotüübi ontoloogia, versioon 2026-09-01: tunnus, selle nimetused, määratlus ja sellega seotud geenid. Lisateave leiab aadressilt hpo.jax.org.
- Andmeversioon 2026.10.16-c6eea6bf.
AtlasKellele me abiks olemeMeie teadusTootedTulemused
Logi sisseKüsiSekveneeri oma genoom↗
From traits to your genome
Read the genes behind these traits in your own DNA.
The Genome Test sequences nearly all of your DNA, not a preset panel, so every gene on these pages is in your data. Premium adds 470+ physician-ready reports.
Alates 449 $
Tasuta kohaletoimetamine · Tulemused 6–8 nädala pärast
